Data / Medical devices / Set, Administration, Intravascular / France
FDA-registered makers of Set, Administration, Intravascular in France: 6 establishments
6 establishments in France are registered with the FDA to make Set, Administration, Intravascular (product code FPA). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Set, Administration, Intravascular
- Product code
- FPA
- Country
- France
Makers of Set, Administration, Intravascular in France
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Cair LGL | Lissieu Rhone, France | Specification developer | 4 | September 1, 2017 | 0 | 0 | 0 | api.fda.gov |
| Cair LGL | Saint Laurent de Chamousset Rhone, France | Manufacturer | 4 | September 1, 2017 | 0 | 0 | 0 | api.fda.gov |
| Vygon S A | ECOUEN 95440 Val-d'Oise, France | Exporter to the US, Manufacturer | 3 | May 2, 2012 | 0 | 0 | 0 | api.fda.gov |
| Perouse Medical | FRANCE Oise, France | Manufacturer | 2 | May 2, 2012 | 0 | 0 | 0 | api.fda.gov |
| Sipa | Avesnes Sur Helpe Hauts-de-France, France | Manufacturer | 1 | September 29, 1988 | 0 | 0 | 0 | api.fda.gov |
| Fresenius Vial S.A.S. | Brezins Isere, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.